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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Fgf9 helps create new hair follicles after injury through skin T cells.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

D-OCT shows increased blood vessel growth in response to tissue damage in Frontal Fibrosing Alopecia and is useful for diagnosis and monitoring.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A substance called FGF9 from certain immune cells can trigger new hair growth during wound healing in mice, but humans may not have the same response due to fewer of these cells.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Cells from concentrated growth factor can become different cell types.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Folliculotropic mycosis fungoides can occur in children and is diagnosed with specific tests, but often stays in early stages with treatment.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Gap junctions help control feather pattern formation in chickens.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Consider NF1 in newborns with rare congenital anomalies.

Certain gene variants can influence acne risk and severity.

FGF-1 causes spiral ganglion neurites to branch more.

An adult had a rare scalp infection in the forehead area, treated successfully with itraconazole.